Evidence map›Paper›PMID 41758177›Full record

ArticlePacific Symposium on Biocomputing. Pacific Symposium on Biocomputing2026

Prototype Learning to Create Refined Interpretable Digital Phenotypes from ECGs.

Sahil Sethi, David Chen, Michael C Burkhart, Nipun Bhandari, Bashar Ramadan, Brett Beaulieu-Jones

Abstract read
In one paragraph

Article in Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Sahil SethiPritzker School of Medicine, University of Chicago, IL, USA2Center for Computational Medicine & Clinical AI, Section of Biomedical Data Science, Department of Medicine, University of Chicago, IL, USA.
David ChenCenter for Computational Medicine & Clinical AI, Section of Biomedical Data Science, Department of Medicine, University of Chicago, IL, USA.
Michael C BurkhartCenter for Computational Medicine & Clinical AI, Section of Biomedical Data Science, Department of Medicine, University of Chicago, IL, USA.
Nipun BhandariDivision of Cardiovascular Medicine, Department of Internal Medicine, University of California Davis, CA, USA.
Bashar RamadanSection of Hospital Medicine, Department of Medicine, University of Chicago, IL, USA.
Brett Beaulieu-JonesCenter for Computational Medicine & Clinical AI, Section of Biomedical Data Science, Department of Medicine, University of Chicago, IL, USA, beaulieujones@uchicago.edu.

Funding

Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Characterizing Population Differences between Clinical Trial and Real World PopulationsR00NS114850 · NINDS · UNIVERSITY OF CHICAGO · PI BEAULIEU-JONES, BRETT K · 2023 to 2025
$740k
NCATS NIH HHS UL1 TR000430NINDS NIH HHS R00 NS114850
6 · The paper itself

Abstract

Prototype-based neural networks offer interpretable predictions by comparing inputs to learned, representative signal patterns anchored in training data. While such models have shown promise in the classification of physiological data, it remains unclear whether their prototypes capture an underlying structure that aligns with broader clinical phenotypes.We use a prototype-based deep learning model trained for multi-label ECG classification using the PTB-XL dataset. Then without modification we performed inference on the MIMIC-IV clinical database. We assess whether individual prototypes, trained solely for classification, are associated with hospital discharge diagnoses in the form of phecodes in this external population. Individual prototypes demonstrate significantly stronger and more specific associations with clinical outcomes compared to the classifier's class predictions, NLP-extracted concepts, or broader prototype classes across all phecode categories. Prototype classes with mixed significance patterns exhibit significantly greater intra-class distances (p < 0.0001), indicating the model learned to differentiate clinically meaningful variations within diagnostic categories. The prototypes achieve strong predictive performance across diverse conditions, with AUCs ranging as high as 0.89 for atrial fibrillation to 0.91 for heart failure, while also showing substantial signal for non-cardiac conditions such as sepsis and renal disease. These findings suggest that prototype-based models can support interpretable digital phenotyping from physiologic time-series data, providing transferable intermediate phenotypes that capture clinically meaningful physiologic signatures beyond their original training objectives.

Indexed as

ElectrocardiographyAtrial FibrillationClassification AlgorithmsComputational BiologyDatabases, FactualDeep LearningDigital HealthHumansMachine LearningNeural Networks, ComputerPhenotypePredictive Learning Models

Identifiers

PMID41758177
PMCPMC12952667

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.